Programmed Nanoparticle‐Loaded Nanoparticles for Deep‐Penetrating 3D Cancer Therapy. Issue 29 (18th May 2018)
- Record Type:
- Journal Article
- Title:
- Programmed Nanoparticle‐Loaded Nanoparticles for Deep‐Penetrating 3D Cancer Therapy. Issue 29 (18th May 2018)
- Main Title:
- Programmed Nanoparticle‐Loaded Nanoparticles for Deep‐Penetrating 3D Cancer Therapy
- Authors:
- Kim, Jinhwan
Jo, Changshin
Lim, Won‐Gwang
Jung, Sungjin
Lee, Yeong Mi
Lim, Jun
Lee, Haeshin
Lee, Jinwoo
Kim, Won Jong - Abstract:
- Abstract: Tumors are 3D, composed of cellular agglomerations and blood vessels. Therapies involving nanoparticles utilize specific accumulations due to the leaky vascular structures. However, systemically injected nanoparticles are mostly uptaken by cells located on the surfaces of cancer tissues, lacking deep penetration into the core cancer regions. Herein, an unprecedented strategy, described as injecting "nanoparticle‐loaded nanoparticles" to address the long‐lasting problem is reported for effective surface‐to‐core drug delivery in entire 3D tumors. The "nanoparticle‐loaded nanoparticle" is a silica nanoparticle (≈150 nm) with well‐developed, interconnected channels (diameter of ≈30 nm), in which small gold nanoparticles (AuNPs) (≈15 nm) with programmable DNA are located. The nanoparticle (AuNPs)‐loaded nanoparticles (silica): (1) can accumulate in tumors through leaky vascular structures by protecting the inner therapeutic AuNPs during blood circulation, and then (2) allow diffusion of the AuNPs for penetration into the entire surface‐to‐core tumor tissues, and finally (3) release a drug triggered by cancer‐characteristic pH gradients. The hierarchical "nanoparticle‐loaded nanoparticle" can be a rational design for cancer therapies because the outer large nanoparticles are effective in blood circulation and in protection of the therapeutic nanoparticles inside, allowing the loaded small nanoparticles to penetrate deeply into 3D tumors with anticancer drugs. Abstract :Abstract: Tumors are 3D, composed of cellular agglomerations and blood vessels. Therapies involving nanoparticles utilize specific accumulations due to the leaky vascular structures. However, systemically injected nanoparticles are mostly uptaken by cells located on the surfaces of cancer tissues, lacking deep penetration into the core cancer regions. Herein, an unprecedented strategy, described as injecting "nanoparticle‐loaded nanoparticles" to address the long‐lasting problem is reported for effective surface‐to‐core drug delivery in entire 3D tumors. The "nanoparticle‐loaded nanoparticle" is a silica nanoparticle (≈150 nm) with well‐developed, interconnected channels (diameter of ≈30 nm), in which small gold nanoparticles (AuNPs) (≈15 nm) with programmable DNA are located. The nanoparticle (AuNPs)‐loaded nanoparticles (silica): (1) can accumulate in tumors through leaky vascular structures by protecting the inner therapeutic AuNPs during blood circulation, and then (2) allow diffusion of the AuNPs for penetration into the entire surface‐to‐core tumor tissues, and finally (3) release a drug triggered by cancer‐characteristic pH gradients. The hierarchical "nanoparticle‐loaded nanoparticle" can be a rational design for cancer therapies because the outer large nanoparticles are effective in blood circulation and in protection of the therapeutic nanoparticles inside, allowing the loaded small nanoparticles to penetrate deeply into 3D tumors with anticancer drugs. Abstract : Programmed nanoparticle‐loaded nanoparticles, comprising large‐pored silica nanoparticles and DNA‐modified gold nanoparticles, exhibit sequential dynamic behavior for cancer therapy with three stages operated by DNA transition: preferential accumulation in the cancerous region, deep penetration into the 3D cancer tissues, and intracellular specific anticancer drug release. … (more)
- Is Part Of:
- Advanced materials. Volume 30:Issue 29(2018)
- Journal:
- Advanced materials
- Issue:
- Volume 30:Issue 29(2018)
- Issue Display:
- Volume 30, Issue 29 (2018)
- Year:
- 2018
- Volume:
- 30
- Issue:
- 29
- Issue Sort Value:
- 2018-0030-0029-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-05-18
- Subjects:
- deep penetration -- DNA engineering -- gold nanoparticle -- large‐pored mesoporous silica nanoparticle -- tumor pH gradient
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-4095 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adma.201707557 ↗
- Languages:
- English
- ISSNs:
- 0935-9648
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.897800
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 6994.xml